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Hemoglobin
international journal for hemoglobin research
Volume 39, 2015 - Issue 6
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Original Article

Diagnosis of a Family with the Novel –α21.9 Thalassemia Deletion

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Pages 419-422 | Received 11 Dec 2014, Accepted 22 Jun 2015, Published online: 07 Sep 2015

References

  • Long J, Yan S, Lao K, et al. The diagnosis and molecular analysis of a novel 21.9kb deletion (Qinzhou type deletion) causing α+ thalassemia. Blood Cells Mol Dis. 2014;52(4):225–229
  • Long J, Ye X, Lao K, et al. Detection of three common α-thalassemia in non-deletion types and six common thalassemia in deletion types by QF-PCR. Clin Biochem. 2013;46(18):1860–1864
  • Wei XF, Shang X, He DQ, et al. Molecular characterization of a novel 27.6-kb deletion causing α+ thalassemia in a Chinese family. Ann Hematol. 2011;90(1):17–22
  • Lin M, Wu JR, Huang Y, et al. Clinical and molecular characterization of a rare 2.4 kb deletion causing α+ thalassemia in a Chinese family. Blood Cells Mol Dis. 2012;49(2):83–84
  • Zhao JB, Zhao L, Fei YJ, et al. A novel α-thalassemia-2 (−2.7-kb) observed in a Chinese patient with Hb H disease. Am J Hematol. 1991;38(3):248–249
  • Harteveld CL, Higgs DR. α-Thalassaemia. Orphanet J Rare Dis. 2010;5:13. doi: 10.1186/1750-1172-5-13

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